Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc8 |
A |
G |
7: 45,754,943 (GRCm39) |
I1525T |
probably benign |
Het |
Agtpbp1 |
A |
G |
13: 59,648,392 (GRCm39) |
V476A |
probably benign |
Het |
Aipl1 |
A |
G |
11: 71,922,256 (GRCm39) |
I151T |
probably benign |
Het |
Atp2a2 |
A |
G |
5: 122,596,554 (GRCm39) |
F855S |
possibly damaging |
Het |
Axdnd1 |
T |
C |
1: 156,223,075 (GRCm39) |
T261A |
possibly damaging |
Het |
Cbfa2t2 |
A |
G |
2: 154,365,900 (GRCm39) |
D370G |
probably damaging |
Het |
Cep350 |
T |
C |
1: 155,736,025 (GRCm39) |
I2964V |
probably damaging |
Het |
Clec16a |
T |
C |
16: 10,386,375 (GRCm39) |
V158A |
probably damaging |
Het |
Col6a5 |
G |
A |
9: 105,741,806 (GRCm39) |
T2371I |
probably damaging |
Het |
Cpne8 |
T |
C |
15: 90,503,929 (GRCm39) |
T79A |
probably damaging |
Het |
Cyp2b13 |
A |
G |
7: 25,780,413 (GRCm39) |
R145G |
probably damaging |
Het |
Disc1 |
G |
A |
8: 125,851,289 (GRCm39) |
W391* |
probably null |
Het |
Dnah8 |
G |
A |
17: 30,941,988 (GRCm39) |
V1745I |
probably damaging |
Het |
Dsp |
T |
C |
13: 38,376,886 (GRCm39) |
V1557A |
probably benign |
Het |
Egfem1 |
T |
A |
3: 29,637,145 (GRCm39) |
Y194N |
probably damaging |
Het |
Eif4a3 |
A |
G |
11: 119,179,705 (GRCm39) |
Y361H |
probably damaging |
Het |
Esd |
T |
A |
14: 74,982,153 (GRCm39) |
S189R |
possibly damaging |
Het |
Fancf |
A |
T |
7: 51,511,196 (GRCm39) |
Y269* |
probably null |
Het |
Fbln2 |
A |
T |
6: 91,248,569 (GRCm39) |
H1078L |
possibly damaging |
Het |
Fbxw13 |
A |
G |
9: 109,010,592 (GRCm39) |
|
probably null |
Het |
Fcgr2b |
A |
T |
1: 170,790,941 (GRCm39) |
V284D |
probably benign |
Het |
Fuz |
G |
A |
7: 44,549,718 (GRCm39) |
G363R |
probably damaging |
Het |
Gas7 |
A |
G |
11: 67,574,234 (GRCm39) |
E403G |
probably damaging |
Het |
Gnl1 |
A |
G |
17: 36,291,581 (GRCm39) |
D49G |
possibly damaging |
Het |
Gucy2g |
A |
G |
19: 55,214,445 (GRCm39) |
V561A |
probably benign |
Het |
H1f7 |
A |
T |
15: 98,154,216 (GRCm39) |
V311E |
unknown |
Het |
Hebp2 |
T |
C |
10: 18,420,122 (GRCm39) |
T104A |
probably benign |
Het |
Ighv1-19 |
T |
A |
12: 114,672,377 (GRCm39) |
Q80L |
probably benign |
Het |
Kctd19 |
T |
A |
8: 106,122,959 (GRCm39) |
|
probably null |
Het |
Kdm3b |
T |
C |
18: 34,955,428 (GRCm39) |
L905P |
probably damaging |
Het |
Klkb1 |
T |
C |
8: 45,735,814 (GRCm39) |
D183G |
probably benign |
Het |
Krt6b |
T |
C |
15: 101,588,460 (GRCm39) |
R67G |
possibly damaging |
Het |
Krt75 |
T |
C |
15: 101,482,248 (GRCm39) |
I7V |
probably benign |
Het |
Lpo |
A |
T |
11: 87,697,751 (GRCm39) |
N685K |
probably benign |
Het |
Mroh7 |
A |
T |
4: 106,538,070 (GRCm39) |
I1202N |
probably benign |
Het |
Muc4 |
T |
A |
16: 32,754,572 (GRCm38) |
M1482K |
probably benign |
Het |
Mylk |
T |
A |
16: 34,791,810 (GRCm39) |
V1494E |
probably damaging |
Het |
Neurl4 |
A |
G |
11: 69,801,913 (GRCm39) |
D17G |
probably damaging |
Het |
Nkx6-3 |
A |
G |
8: 23,647,725 (GRCm39) |
Y228C |
probably damaging |
Het |
Nprl2 |
G |
A |
9: 107,420,273 (GRCm39) |
|
probably null |
Het |
Nxf1 |
A |
G |
19: 8,739,669 (GRCm39) |
|
probably null |
Het |
Or4a39 |
A |
G |
2: 89,236,770 (GRCm39) |
F218L |
probably benign |
Het |
Or52u1 |
A |
T |
7: 104,237,730 (GRCm39) |
N240Y |
probably damaging |
Het |
Pde3b |
A |
G |
7: 114,118,847 (GRCm39) |
E662G |
possibly damaging |
Het |
Plekhm3 |
G |
A |
1: 64,977,078 (GRCm39) |
R131C |
probably damaging |
Het |
Plpp7 |
T |
C |
2: 31,985,950 (GRCm39) |
S43P |
probably benign |
Het |
Pramel5 |
A |
G |
4: 143,998,187 (GRCm39) |
L352P |
probably damaging |
Het |
Prepl |
T |
C |
17: 85,395,902 (GRCm39) |
S27G |
probably benign |
Het |
Ptprd |
A |
G |
4: 76,051,542 (GRCm39) |
I227T |
probably damaging |
Het |
Pttg1ip |
C |
T |
10: 77,419,854 (GRCm39) |
Q6* |
probably null |
Het |
Rgl1 |
C |
T |
1: 152,424,813 (GRCm39) |
|
probably null |
Het |
Riiad1 |
C |
A |
3: 94,380,173 (GRCm39) |
G41* |
probably null |
Het |
Rnf214 |
C |
T |
9: 45,807,486 (GRCm39) |
R239H |
probably damaging |
Het |
Rpap3 |
C |
T |
15: 97,584,407 (GRCm39) |
V346I |
probably benign |
Het |
Scaf4 |
G |
A |
16: 90,048,831 (GRCm39) |
Q328* |
probably null |
Het |
Sec23a |
A |
G |
12: 59,051,274 (GRCm39) |
|
probably null |
Het |
Slc5a8 |
T |
A |
10: 88,740,774 (GRCm39) |
|
probably null |
Het |
Slc9a8 |
A |
G |
2: 167,288,449 (GRCm39) |
T183A |
probably benign |
Het |
Sod3 |
A |
T |
5: 52,525,736 (GRCm39) |
H145L |
probably damaging |
Het |
Sp4 |
A |
G |
12: 118,263,341 (GRCm39) |
V235A |
probably damaging |
Het |
Spp1 |
A |
C |
5: 104,588,153 (GRCm39) |
E185A |
possibly damaging |
Het |
Susd1 |
A |
T |
4: 59,351,679 (GRCm39) |
W461R |
probably benign |
Het |
Svil |
A |
C |
18: 5,095,516 (GRCm39) |
K1124Q |
probably damaging |
Het |
Tdrd12 |
A |
T |
7: 35,186,720 (GRCm39) |
|
probably null |
Het |
Terb1 |
A |
T |
8: 105,221,795 (GRCm39) |
N168K |
probably benign |
Het |
Tnnt1 |
A |
G |
7: 4,510,573 (GRCm39) |
L216P |
probably damaging |
Het |
Ttc28 |
A |
G |
5: 111,424,121 (GRCm39) |
K1463E |
probably damaging |
Het |
Twf2 |
T |
G |
9: 106,089,098 (GRCm39) |
|
probably null |
Het |
Urb1 |
C |
T |
16: 90,602,299 (GRCm39) |
R90Q |
probably damaging |
Het |
Wdr45b |
A |
T |
11: 121,219,650 (GRCm39) |
C299* |
probably null |
Het |
Wrap73 |
A |
G |
4: 154,237,138 (GRCm39) |
S54G |
probably damaging |
Het |
Zeb2 |
T |
C |
2: 44,888,931 (GRCm39) |
K323R |
probably damaging |
Het |
Zfp410 |
T |
C |
12: 84,378,582 (GRCm39) |
I302T |
possibly damaging |
Het |
|
Other mutations in Apc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00507:Apc
|
APN |
18 |
34,449,979 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00898:Apc
|
APN |
18 |
34,450,147 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01111:Apc
|
APN |
18 |
34,448,189 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01347:Apc
|
APN |
18 |
34,450,723 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01375:Apc
|
APN |
18 |
34,446,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01805:Apc
|
APN |
18 |
34,451,271 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01997:Apc
|
APN |
18 |
34,448,476 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02033:Apc
|
APN |
18 |
34,443,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02323:Apc
|
APN |
18 |
34,448,863 (GRCm39) |
nonsense |
probably null |
|
IGL02373:Apc
|
APN |
18 |
34,449,212 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02379:Apc
|
APN |
18 |
34,431,798 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02456:Apc
|
APN |
18 |
34,446,935 (GRCm39) |
nonsense |
probably null |
|
IGL02552:Apc
|
APN |
18 |
34,446,035 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02676:Apc
|
APN |
18 |
34,448,687 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02756:Apc
|
APN |
18 |
34,447,588 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02938:Apc
|
APN |
18 |
34,448,281 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02974:Apc
|
APN |
18 |
34,401,436 (GRCm39) |
splice site |
probably benign |
|
IGL03124:Apc
|
APN |
18 |
34,433,038 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03201:Apc
|
APN |
18 |
34,445,429 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03339:Apc
|
APN |
18 |
34,431,527 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Apc
|
UTSW |
18 |
34,415,050 (GRCm39) |
intron |
probably benign |
|
FR4342:Apc
|
UTSW |
18 |
34,415,052 (GRCm39) |
intron |
probably benign |
|
FR4449:Apc
|
UTSW |
18 |
34,415,058 (GRCm39) |
intron |
probably benign |
|
FR4449:Apc
|
UTSW |
18 |
34,415,053 (GRCm39) |
intron |
probably benign |
|
FR4548:Apc
|
UTSW |
18 |
34,415,051 (GRCm39) |
intron |
probably benign |
|
FR4737:Apc
|
UTSW |
18 |
34,415,052 (GRCm39) |
intron |
probably benign |
|
FR4976:Apc
|
UTSW |
18 |
34,415,057 (GRCm39) |
nonsense |
probably null |
|
FR4976:Apc
|
UTSW |
18 |
34,415,053 (GRCm39) |
intron |
probably benign |
|
FR4976:Apc
|
UTSW |
18 |
34,415,051 (GRCm39) |
intron |
probably benign |
|
R0385:Apc
|
UTSW |
18 |
34,448,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R0535:Apc
|
UTSW |
18 |
34,394,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R0561:Apc
|
UTSW |
18 |
34,446,356 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0590:Apc
|
UTSW |
18 |
34,449,283 (GRCm39) |
nonsense |
probably null |
|
R0626:Apc
|
UTSW |
18 |
34,451,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R0991:Apc
|
UTSW |
18 |
34,449,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R1564:Apc
|
UTSW |
18 |
34,448,202 (GRCm39) |
missense |
probably benign |
0.00 |
R1663:Apc
|
UTSW |
18 |
34,401,378 (GRCm39) |
missense |
probably damaging |
0.98 |
R1737:Apc
|
UTSW |
18 |
34,450,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Apc
|
UTSW |
18 |
34,445,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Apc
|
UTSW |
18 |
34,450,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1887:Apc
|
UTSW |
18 |
34,405,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R1957:Apc
|
UTSW |
18 |
34,450,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R1974:Apc
|
UTSW |
18 |
34,433,057 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2005:Apc
|
UTSW |
18 |
34,443,962 (GRCm39) |
critical splice donor site |
probably null |
|
R2013:Apc
|
UTSW |
18 |
34,448,644 (GRCm39) |
missense |
probably damaging |
0.98 |
R2014:Apc
|
UTSW |
18 |
34,448,644 (GRCm39) |
missense |
probably damaging |
0.98 |
R2015:Apc
|
UTSW |
18 |
34,448,644 (GRCm39) |
missense |
probably damaging |
0.98 |
R2017:Apc
|
UTSW |
18 |
34,446,655 (GRCm39) |
missense |
probably benign |
0.00 |
R2056:Apc
|
UTSW |
18 |
34,449,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Apc
|
UTSW |
18 |
34,402,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R2120:Apc
|
UTSW |
18 |
34,409,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Apc
|
UTSW |
18 |
34,445,098 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2133:Apc
|
UTSW |
18 |
34,445,098 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2291:Apc
|
UTSW |
18 |
34,445,544 (GRCm39) |
missense |
probably benign |
0.45 |
R2332:Apc
|
UTSW |
18 |
34,450,112 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2360:Apc
|
UTSW |
18 |
34,394,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R2407:Apc
|
UTSW |
18 |
34,447,315 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2507:Apc
|
UTSW |
18 |
34,449,590 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2940:Apc
|
UTSW |
18 |
34,409,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R3404:Apc
|
UTSW |
18 |
34,446,655 (GRCm39) |
missense |
probably benign |
0.00 |
R3411:Apc
|
UTSW |
18 |
34,402,312 (GRCm39) |
splice site |
probably benign |
|
R3778:Apc
|
UTSW |
18 |
34,446,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R3826:Apc
|
UTSW |
18 |
34,412,388 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4599:Apc
|
UTSW |
18 |
34,451,040 (GRCm39) |
nonsense |
probably null |
|
R4611:Apc
|
UTSW |
18 |
34,451,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R4664:Apc
|
UTSW |
18 |
34,431,647 (GRCm39) |
missense |
probably damaging |
0.98 |
R5007:Apc
|
UTSW |
18 |
34,446,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R5066:Apc
|
UTSW |
18 |
34,449,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Apc
|
UTSW |
18 |
34,449,162 (GRCm39) |
nonsense |
probably null |
|
R5259:Apc
|
UTSW |
18 |
34,447,343 (GRCm39) |
missense |
probably benign |
0.29 |
R5440:Apc
|
UTSW |
18 |
34,354,213 (GRCm39) |
unclassified |
probably benign |
|
R5508:Apc
|
UTSW |
18 |
34,431,633 (GRCm39) |
missense |
probably damaging |
0.97 |
R5512:Apc
|
UTSW |
18 |
34,443,962 (GRCm39) |
critical splice donor site |
probably benign |
|
R5850:Apc
|
UTSW |
18 |
34,451,116 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5951:Apc
|
UTSW |
18 |
34,450,199 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5966:Apc
|
UTSW |
18 |
34,354,140 (GRCm39) |
utr 5 prime |
probably benign |
|
R6081:Apc
|
UTSW |
18 |
34,423,164 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6116:Apc
|
UTSW |
18 |
34,449,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6351:Apc
|
UTSW |
18 |
34,445,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R6354:Apc
|
UTSW |
18 |
34,445,581 (GRCm39) |
missense |
probably benign |
0.02 |
R6467:Apc
|
UTSW |
18 |
34,402,252 (GRCm39) |
missense |
probably benign |
0.22 |
R6974:Apc
|
UTSW |
18 |
34,431,480 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7027:Apc
|
UTSW |
18 |
34,445,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R7096:Apc
|
UTSW |
18 |
34,449,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R7289:Apc
|
UTSW |
18 |
34,448,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R7439:Apc
|
UTSW |
18 |
34,445,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R7441:Apc
|
UTSW |
18 |
34,445,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R7534:Apc
|
UTSW |
18 |
34,450,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R7685:Apc
|
UTSW |
18 |
34,447,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R7814:Apc
|
UTSW |
18 |
34,405,592 (GRCm39) |
missense |
probably damaging |
0.98 |
R7954:Apc
|
UTSW |
18 |
34,447,321 (GRCm39) |
missense |
probably damaging |
0.99 |
R8352:Apc
|
UTSW |
18 |
34,445,804 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8452:Apc
|
UTSW |
18 |
34,445,804 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8497:Apc
|
UTSW |
18 |
34,446,083 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8545:Apc
|
UTSW |
18 |
34,450,084 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8554:Apc
|
UTSW |
18 |
34,445,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R8955:Apc
|
UTSW |
18 |
34,401,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R9014:Apc
|
UTSW |
18 |
34,354,074 (GRCm39) |
start gained |
probably benign |
|
R9061:Apc
|
UTSW |
18 |
34,446,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Apc
|
UTSW |
18 |
34,450,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Apc
|
UTSW |
18 |
34,447,040 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9521:Apc
|
UTSW |
18 |
34,445,738 (GRCm39) |
missense |
probably benign |
0.24 |
R9546:Apc
|
UTSW |
18 |
34,445,311 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9547:Apc
|
UTSW |
18 |
34,445,311 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9557:Apc
|
UTSW |
18 |
34,451,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R9592:Apc
|
UTSW |
18 |
34,443,823 (GRCm39) |
nonsense |
probably null |
|
R9675:Apc
|
UTSW |
18 |
34,449,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R9736:Apc
|
UTSW |
18 |
34,450,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R9792:Apc
|
UTSW |
18 |
34,447,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R9793:Apc
|
UTSW |
18 |
34,447,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R9795:Apc
|
UTSW |
18 |
34,447,628 (GRCm39) |
missense |
probably damaging |
1.00 |
RF046:Apc
|
UTSW |
18 |
34,415,062 (GRCm39) |
critical splice donor site |
probably benign |
|
RF063:Apc
|
UTSW |
18 |
34,415,062 (GRCm39) |
critical splice donor site |
probably benign |
|
X0021:Apc
|
UTSW |
18 |
34,445,161 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Apc
|
UTSW |
18 |
34,445,429 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Apc
|
UTSW |
18 |
34,446,220 (GRCm39) |
nonsense |
probably null |
|
Z1177:Apc
|
UTSW |
18 |
34,447,516 (GRCm39) |
missense |
probably benign |
0.06 |
|